Autosomal Dominant | Brittle Bone Disorders

Skip to main content

Search

Join Our Contact Registry

Header Social Media

Our Research
Patient and Families
Researchers and Clinicians
Early Stage Investigators
News and Events
About Us

An NIH-Funded Rare Diseases Clinical Research Network Consortium

Describes a genetic disorder such as OI that is caused by a gene that is not linked to a sex chromosome and that is cause by a single abnormal gene.

Footer menu

Web Policies
Rare Diseases Clinical Research Network
Genetic and Rare Diseases Information Center
Members Login
Contact Us
Sitemap

The Brittle Bone Disorders Consortium (BBDC) is part of the Rare Diseases Clinical Research Network (RDCRN), which is funded by the National Institutes of Health (NIH) and led by the National Center for Advancing Translational Sciences (NCATS) through its Division of Rare Diseases Research Innovation (DRDRI). BBDC is funded under grant number U54AR068069 as a collaboration between NCATS, the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), the National Institute of Dental and Craniofacial Research (NIDCR), the National Human Genome Research Institute (NHGRI), the Office of Research on Women’s Health (ORWH), and the NIH Office of the Director (OD). This website is hosted by the network’s Data Management and Coordinating Center at Cincinnati Children’s Hospital Medical Center, which is funded by NCATS and the National Institute of Neurological Disorders and Stroke (NINDS) under grant number TR002818. The content of this website is solely the responsibility of the BBDC administrative coordinating center at Baylor College of Medicine and does not necessarily represent the official views of the NIH.

social media